MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-10 for FIBER OPTIC ILLUMINATOR 8065751577 manufactured by Alcon Research, Ltd. - Houston.
[92748654]
A product sample has been received by the manufacturer and it is awaiting evaluation. A supplemental mdr will be filed as necessary in accordance with 21 cfr 803. 56 when additional reportable information becomes available. The manufacturer internal reference number is: (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[92748655]
A surgeon reported an infusion cannula was inserted into a broken trocar cannula and an irrigation failure occurred which caused an ocular hypotony during a procedure. The procedure was completed without product replacement. There was no harm to the patient. No additional information is expected.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1644019-2017-00791 |
MDR Report Key | 7017995 |
Date Received | 2017-11-10 |
Date of Report | 2018-02-01 |
Date of Event | 2017-10-12 |
Date Mfgr Received | 2018-01-08 |
Device Manufacturer Date | 2017-04-19 |
Date Added to Maude | 2017-11-10 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. NADIA BAILEY |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152230 |
Manufacturer G1 | ALCON RESEARCH, LTD. - HOUSTON |
Manufacturer Street | 9965 BUFFALO SPEEDWAY |
Manufacturer City | HOUSTON TX 77054 |
Manufacturer Country | US |
Manufacturer Postal Code | 77054 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 0 |
Brand Name | FIBER OPTIC ILLUMINATOR |
Generic Name | LIGHT, SURGICAL, FIBEROPTIC |
Product Code | FST |
Date Received | 2017-11-10 |
Returned To Mfg | 2017-11-08 |
Model Number | NA |
Catalog Number | 8065751577 |
Lot Number | 2005823H |
Device Expiration Date | 2019-03-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON RESEARCH, LTD. - HOUSTON |
Manufacturer Address | 9965 BUFFALO SPEEDWAY HOUSTON TX 77054 US 77054 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-11-10 |